Manufacturing Supervisor

Manufacturing Supervisor – DPI (1st, 2nd, or 3rd Shift)

Work Location: Hauppauge, NY
Employment: Full-Time | On-Site
Industry: Regulated Manufacturing

A large regulated pharmaceutical manufacturing facility in Hauppauge, NY is seeking a Manufacturing Supervisor (Dry Powder Inhalation – DPI) to lead operations on the production floor. This role will supervise teams, support production schedules, champion safety and quality standards, and ensure compliance with cGMP guidelines.

Position Summary

This role oversees daily operations of DPI manufacturing and supports product development, commercial production, documentation, and safety compliance. The Supervisor will lead a team of operators and collaborate with cross-functional departments to achieve manufacturing schedules and maintain product quality.

Key Responsibilities

• Lead and supervise manufacturing activities for DPI products in a cleanroom/controlled environment
• Assign tasks, support daily troubleshooting, and ensure adherence to SOPs and cGMP
• Review batch manufacturing records and support investigations, deviations, and documentation
• Coordinate with QA, QC, R&D, Maintenance, Supply Chain, and other departments
• Support validation batches, bio-batch execution, and technical transfers
• Enforce safety procedures, equipment cleaning, and facility standards
• Train and evaluate employees based on performance expectations and policy guidelines
• Participate in audits, compliance reviews, and regulatory inspections
• Monitor productivity, equipment performance, and process improvements
• Maintain accurate technical documentation and compliant records
• Support extended working hours or weekends if required by production demand

Required Qualifications

✔ Bachelor’s or Master’s degree in Pharmaceutical Sciences, Pharmaceutical Engineering, or related fields
✔ 1–3 years of hands-on experience in pharmaceutical or regulated manufacturing
✔ Strong understanding of cGMP, SOPs, compliance, documentation, quality & safety
✔ Ability to investigate deviations and support root cause analysis
✔ Proficiency in Microsoft Office; familiarity with SAP is a plus

Preferred Background

• Pharmaceutical / Biopharmaceutical Manufacturing
• Medical Device / Sterile Manufacturing
• Respiratory Technology Products (MDI, DPI preferred)
• FDA/USP/GMP-Regulated Production

Work Schedule

• Primary Opening: 2nd Shift
• Additional shifts may be available (1st, 2nd, or 3rd) based on business needs
• Extended workweeks (Saturdays/Sundays/holidays) may be required

Note: This role is fully on-site; remote work is not available.

Benefits Overview (Company Policy Applies)

• Medical, Dental, Vision insurance
• 401(k) with company match
• HSA / FSA Programs
• PTO (Vacation / Sick / Flex Days / Holidays)
• Disability, Parental Leave, Family Leave
• Employee Discounts & additional corporate benefits

Job Type: Full-time

Benefits:

• 401(k) matching
• Dental insurance
• Employee assistance program
• Employee discount
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance
• Vision insurance

Application Question(s):

• What are your preferred hours or best time for a phone call?

• What is your work authorization/ Work Permit / Visa Status in the USA?

• Are you based nearby Hauppauge, New York; or are you willing to relocate to Hauppauge, New York for this position? Please share your location. (City, State & Zip code)

• Please share your regular email and regular phone number.

• What is your expected annual base salary for this position?

• Which shift(s) are you willing to work? (1st/ 2nd/ 3rd/ Any available shift)

• How many years of experience do you have in pharmaceutical or regulated manufacturing?
• Do you have supervisory or lead experience in manufacturing? if yes, How many years & Where?
• What is your highest educational qualification? Please specify with years of completion.

Work Location: On the road